Clinical Research Coord I

Job description

Overview Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator I is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for research protocols related to treatment, ancillary services, and prevention practices. Responsibilities: - Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAA - Identify, schedule and/or conduct participant study visits, interviews, and tests - Coordinate participant remuneration/compensation per protocol - Maintain all regulatory documentation, including local or central IRB and study data. Provide data/support to study Investigators, sponsors and/or external monitors/auditors - Identify issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance - Document and collect data and/or samples for research related procedures performed during participant study visits. - Ensure clinicians and/or PI accurately document their study...